Propping P - Search Results

1

Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis.

Lamberti C, Jungck M, Laarmann M, Knapp M, Caspari R, Friedl W, Sauerbruch T, Propping P, Kruse R. Lamberti C, et al. Among authors: propping p. Pharmacogenetics. 2002 Jan;12(1):49-54. doi: 10.1097/00008571-200201000-00007. Pharmacogenetics. 2002. PMID: 11773864

2

Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.

Aretz S, Uhlhaas S, Sun Y, Pagenstecher C, Mangold E, Caspari R, Möslein G, Schulmann K, Propping P, Friedl W. Aretz S, et al. Among authors: propping p. Hum Mutat. 2004 Nov;24(5):370-80. doi: 10.1002/humu.20087. Hum Mutat. 2004. PMID: 15459959

3

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.

Aretz S, Uhlhaas S, Caspari R, Mangold E, Pagenstecher C, Propping P, Friedl W. Aretz S, et al. Among authors: propping p. Eur J Hum Genet. 2004 Jan;12(1):52-8. doi: 10.1038/sj.ejhg.5201088. Eur J Hum Genet. 2004. PMID: 14523376

4

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis.

Mandl M, Paffenholz R, Friedl W, Caspari R, Sengteller M, Propping P. Mandl M, et al. Among authors: propping p. Hum Mol Genet. 1994 Jan;3(1):181-4. doi: 10.1093/hmg/3.1.181. Hum Mol Genet. 1994. PMID: 8162022

5

Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC protein.

Friedl W, Meuschel S, Caspari R, Lamberti C, Krieger S, Sengteller M, Propping P. Friedl W, et al. Among authors: propping p. Hum Genet. 1996 May;97(5):579-84. doi: 10.1007/BF02281864. Hum Genet. 1996. PMID: 8655134

6

Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer.

Lamberti C, Kruse R, Ruelfs C, Caspari R, Wang Y, Jungck M, Mathiak M, Malayeri HR, Friedl W, Sauerbruch T, Propping P. Lamberti C, et al. Among authors: propping p. Gut. 1999 Jun;44(6):839-43. doi: 10.1136/gut.44.6.839. Gut. 1999. PMID: 10323887 Free PMC article.

7

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.

Friedl W, Caspari R, Sengteller M, Uhlhaas S, Lamberti C, Jungck M, Kadmon M, Wolf M, Fahnenstich J, Gebert J, Möslein G, Mangold E, Propping P. Friedl W, et al. Among authors: propping p. Gut. 2001 Apr;48(4):515-21. doi: 10.1136/gut.48.4.515. Gut. 2001. PMID: 11247896 Free PMC article.

8

Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?

Aretz S, Koch A, Uhlhaas S, Friedl W, Propping P, von Schweinitz D, Pietsch T. Aretz S, et al. Among authors: propping p. Pediatr Blood Cancer. 2006 Nov;47(6):811-8. doi: 10.1002/pbc.20698. Pediatr Blood Cancer. 2006. PMID: 16317745

9

MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype.

Aretz S, Uhlhaas S, Goergens H, Siberg K, Vogel M, Pagenstecher C, Mangold E, Caspari R, Propping P, Friedl W. Aretz S, et al. Among authors: propping p. Int J Cancer. 2006 Aug 15;119(4):807-14. doi: 10.1002/ijc.21905. Int J Cancer. 2006. PMID: 16557584

10

Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).

Aretz S, Stienen D, Friedrichs N, Stemmler S, Uhlhaas S, Rahner N, Propping P, Friedl W. Aretz S, et al. Among authors: propping p. Hum Mutat. 2007 Oct;28(10):985-92. doi: 10.1002/humu.20549. Hum Mutat. 2007. PMID: 17486639

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